Canonical Allele Identifier: CA659845271
Gene: RBM20 HGNC NCBI

Linked Data

dbSNP Id: rs1183511005
gnomAD v4: 10-110644306-CCTCCTCCCCGCCCCTCGCGT-C
MyVariant Identifiers: chr10:g.112404065_112404084del (hg19) chr10:g.110644307_110644326del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.110644318_110644337del , CM000672.2:g.110644318_110644337del GRCh38
NC_000010.10:g.112404076_112404095del , CM000672.1:g.112404076_112404095del GRCh37
NC_000010.9:g.112394066_112394085del NCBI36
NG_021177.1:g.4922_4941del , LRG_382:g.4922_4941del

Transcript Alleles

HGVS Amino-acid Change
XM_017016103.2:c.26+878_26+897del XP_016871592.1:n.26+878_26+897del
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